The present invention relates a new process to synthesize 6-(7-((1-aminocyclo-propyl)-methoxy)-6-methoxyquinolin-4-yloxy)-N-methyl-1-naphthamide (AL3810) by deprotection of substituted benzyl 1-((6-methoxy-4-(5-(methylcarbamoyl)naphthalen-2-yloxy)quinolin-7-yloxy)-methyl)cyc-lopropylcarbamate (Formula I) under a diluted or weak acidic condition. A stable crystalline form of 6-(7-((1-aminocyclo-propyl)-methoxy)-6-methoxyquinolin-4-yloxy)-N-methyl-1-naphthamide has also been prepared.
##STR00001##
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1. A crystalline form of 6-(7-((1-aminocyclopropyl)methoxy)-6-methoxyquinolin-4-yloxy)-N-methyl-1-naphthamide exhibiting at least one of following properties:
a melting point at 192° C.-196° C.; a dsc having observable endotherm from about 193° C.-202° C.;
a tga demonstrating as an unsolvated material with weight loss at about 230° C.;
a xrpd having pattern comprising characteristic peaks with all intensity % expressed in d values and angles or similar values and angles as follows:
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This application claims the benefit of U.S. Provisional Applications 61/754,516 filed on Jan. 18, 2013
The present invention relates a new process to synthesize 6-(7-((1-aminocyclo-propyl)-methoxy)-6-methoxyquinolin-4-yloxy)-N-methyl-1-naphthamide (AL3810) by deprotection of substituted benzyl 1-((6-methoxy-4-(5-(methylcarbamoyl)naphthalen-2-yloxy)quinolin-7-yloxy)-methyl)cyclopropylcarbamate (Formula I) under a diluted or weak acidic condition. A stable crystalline form of 6-(7-((1-aminocyclo-propyl)-methoxy)-6-methoxyquinolin-4-yloxy)-N-methyl-1-naphthamide has also been prepared.
6-(7-((1-Aminocyclopropyl)-methoxy)-6-methoxyquinolin-4-yloxy)-N-methyl-1-naphthamide (AL3810), or a pharmaceutically acceptable salt (such as hydrochloride salt) thereof, has been developed as an anti-tumor agent also named as E3810 and lucitanib, see “Journal of Cellular and Molecular Medicine vol. 16 issue 10 Oct. 2012. p. 2321-2330”, “Cancer Res Feb. 15, 2011 vol. 71 no. 4 1396-1405”.
This compound has been structurally disclosed in WO2008112408 as an agiogenesis inhibitor with few preparation methods. A new process has been disclosed in WO2010105761 with the removal of use of sodium azide. Both above disclosed processes have involved a deprotection of benzyl carbamate protected precursor by HBr/Acetic acid solution that is a strong, fuming and high corrosive acidic condition. No crystalline form has been disclosed.
The following abbreviations are used and have the meaning below for ease of reference. EtOH: ethanol, MeOH: methanol, IPA: isopropanol, EtOAc: ethyl acetate, RT: room temperature, DIPEA: diisopropylethylamine, DCM: Dichloromethane, DMF: N,N-dimethylformamide, NMP: 1-Methyl-2-pyrrolidinone, ACN: acetonitrile, DEAD: Diethyl azodicarboxylate, DIAD: Diisopropyl azodicarboxylate, CDI: 1,1′-Carbonyldiimidazole, MeNH2.HCl: methylamine hydrochloride, TSA.H2O: 4-toluensulfonic acid monohydrate, DMAP: 4-N,N-dimethylaminopyridine, MsCl: methanesulfonyl chloride, THF: tetrahydrofuran, TFA: trifluoroacetic acid, TEA: triethylamine, DPPA: diphenyl phosphoryl azide,
eq: equivalent, g: gram, mg: milligram, ml: milliliter, min: minutes
The term “halogen”, as used herein, unless otherwise indicated, includes fluoro, chloro, bromo or iodo. such as fluoro and chloro.
The term “halogeno-C1-C6alkyl”, as used herein, unless otherwise indicated, includes 1 to 6 halogen substituted alkyl, such as trifluoromethyl.
The term “C1-C6alkyl”, as used herein, unless otherwise indicated, includes 1 to 6 saturated monovalent hydrocarbon radicals having straight or branched moieties, including, but not limited to, methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, tert-butyl, and the like.
The term “C1-C6alkoxy”, as used herein, unless otherwise indicated, includes —OC1-C6alkyl groups wherein C1-C6alkyl is as defined above, such as methoxy and ethoxy.
The term “cyano”, as used herein, unless otherwise indicated, includes —C—N.
The term “nitro”, as used herein, unless otherwise indicated, includes —NO2.
Methods of Preparation
The present invention relates to a process for preparing 6-(7-((1-aminocyclopropyl)-methoxy)-6-methoxyquinolin-4-yloxy)-N-methyl-1-naphthamide (AL3810) by deprotection of substituted benzyl 1-((6-methoxy-4-(5-(methylcarbamoyl)naphthalen-2-yloxy)quinolin-7-yloxy)-methyl)cyclopropylcarbamate Formula I under a diluted or weak acidic condition according to Process A.
##STR00002##
Wherein
R1 is selected from H, halogen, halogeno-C1-C6alkyl, C1-C6alkyl, C1-C6alkoxy, cyano or nitro;
R2 is selected from C1-C6alkoxy, or nitro.
The present invention relates to the compound of Formula I.
The present invention relates to the methods of preparing a compound having the Formula I.
The present invention also relates to various intermediates useful in the preparation of a compound having the Formula I, and the present invention further relates to the methods of preparing such intermediates.
The present invention relates to the methods of preparing a crystalline form of 6-(7-((1-aminocyclopropyl)-methoxy)-6-methoxyquinolin-4-yloxy)-N-methyl-1-naphthamide.
The present invention relates to a process for preparing 6-(7-((1-aminocyclo-propyl)-methoxy)-6-methoxyquinolin-4-yloxy)-N-methyl-1-naphthamide (AL3810) by deprotection of substituted benzyl 1-((6-methoxy-4-(5-(methylcarbamoyl)naphthalen-2-yloxy)quinolin-7-yloxy)-methyl)cyclopropylcarbamate Formula I under a diluted or weak acidic condition according to above Process A.
Wherein
R1 is selected from H, halogen, halogeno-C1-C6alkyl, C1-C6alkyl, C1-C6alkoxy, cyano or nitro; preferably selected from H, C1-C6alkoxy, or nitro;
R2 is selected from C1-C6alkoxy, or nitro; preferably R2 is methoxy.
A diluted or weak acidic condition is selected from 5-50% TFA in CH2Cl2 or CH3CN, 10% HCl in ethanol, 4NHCl in dioxane, HCOOH in CH3CN or p-toluenesulfonic acid monohydrate in CH3CN; preferably the acid is 10% TFA in CH2Cl2.
The total volume ratio of solvent to reactant is from 2 to 20 folds by weight. The reaction temperature is selected from 0 to 80° C. and the reaction time is selected from 0.5 to 24 hours.
A preferred procedure is shown in Scheme I.
The present invention relates to a process for preparing 6-(7-((1-aminocyclo-propyl)-methoxy)-6-methoxyquinolin-4-yloxy)-N-methyl-1-naphthamide (AL3810) by deprotection of 4-methoxybenzyl 1-((6-methoxy-4-(5-(methylcarbamoyl)naphthalen-2-yloxy)-quinolin-7-yloxy)-methyl)cyclopropylcarbamate Formula II according to Process B.
##STR00003##
The present invention relates to the compound of Formula II.
The present invention relates to the methods of preparing a compound having the Formula II.
The present invention also relates to various intermediates useful in the preparation of a compound having the Formula II, and the present invention further relates to the methods of preparing such intermediates.
Process B of the invention comprises preparing AL3810, a preferred procedure is shown in Scheme II via:
(a) under a condition of 10% TFA in CH2Cl2, preferably at 0° C. to 50° C. for 3-10 hours with 5-20 folds volume of 10% TFA in CH2Cl2 as the solvent, or
(b) under a condition of 2-4 eq TSA.H2O, preferably at room temperature to 80° C. for 10-24 hours with CH3CN as the solvent.
The present invention relates to a compound of Formula I or Formula II and the method preparing Formula I or Formula II according to Process C.
##STR00004##
##STR00005##
Wherein
R1 is selected from H, halogen, halogeno-C1-C6alkyl, C1-C6alkyl, C1-C6alkoxy, cyano or nitro;
R2 is selected from C1-C6alkoxy, or nitro.
Process C of the invention comprises preparing Formula I, a preferred procedure is shown in Scheme III via the reaction between formula 14 and Formula VI using a base, such as: Na2CO3, Cs2CO3 or K2CO3, or between formula 14 and Formula V using a base, such as: Na2CO3, Cs2CO3 or K2CO3, and KI or NAI to give Formula I, preferably the reaction is at a heated condition, such as 60-120° C. in acetone, DMF or NMP.
Formula 14 can be prepared by following steps:
(a) A direct acylation of formula 10 without any protection by methylamine hydrochloride with heat pre-activation of formula 10 at the presence of CDI gives formula 11, preferably the reaction is carried out in DMF or dioxane for 2-8 hours with 1.5-4 eq CDI at a heated condition, such as at 50-120° C.,
(b) (i) Coupling formula 11 with formula 12 (WO2008112408) at 100-160° C. in lutidine, such as 1,6-lutidine, or pyridine with 1.5-3 eq DMAP for 2-24 hours gives formula 13, or
(ii) Coupling formula 11 with formula 12 under similar Ullmann reaction conditions, such as: a base, CuI and 2-picolinic acid gives formula 13, preferably a base is one of Na2CO3, Cs2CO3 and K2CO3, CuI amount is catalytic amount at 1-50% eq and 2-piclinic acid is at 1-50% eq. The reaction is at 100-160° C. in DMF or NMP for 10-36 hours, or
(iii) Coupling formula 11 with formula 12 under similar Ullmann reaction conditions, such as: a base, CuI and pentanedione gives formula 13, preferably a base is one of Na2CO3, Cs2CO3 and K2CO3, CuI amount is catalytic amount at 1-50% eq and pentanedione is 1,4-pentanedione. The reaction is at 100-160° C. in DMF or NMP for 10-36 hours.
(c) Deprotecting formula 13 with TFA gives formula 14 as a TFA salt, preferably at 60-100° C. for 0.5-8 hours.
Formula VI or Formula V can be prepared by following steps:
(d) Reacting formula 15 with R1, R2 substituted benzyl alcohol with DPPA and triethylamine gives Formula III, preferably using 2-4 eq DPPA and 2-4 eq TEA in toluene or dioxane at a heated condition for 10-28 hours through Curtis rearrangement.
(e) Reducting Formula III by NaBH4 gives Formula IV, preferably at reflux condition in THF with addition of methanol.
(f) Reacting Formula IV with CH3SO2Cl gives Formula V, preferably in a basic condition at −10° C.-25° C.
(g) Reacting Formula V with KI or NaI gives Formula VI, preferably refluxing in acetone or acetonitrile. This step can be modified as one pot reaction without isolation as Scheme III described.
Process C of the invention comprises preparing Formula II, a preferred procedure is shown in Scheme IV via the reaction between formula 14 and formula 15f using a base, such as: Na2CO3, Cs2CO3 or K2CO3, or between formula 14 and formula 15d using a base, such as: Na2CO3, Cs2CO3 or K2CO3, and KI or NaI at a heated condition, such as at 60-120° C. of one pot reaction in acetone, DMF or NMP to give Formula II.
The present invention relates to the compound of Formula I and the method preparing Formula I according to Process D.
##STR00006##
Process D of the invention comprises preparing Formula I, a preferred procedure is shown in Scheme V via acylazide formula 17 reacting with R1, R2 substituted benzyl alcohol in a heated condition, preferably toulene or dioxane refluxing condition.
Formula 17 can be prepared by reacting formula 16 with ethyl chloroformate at 0° C. in DMF or THF at the presence of TEA or DIPEA to form a mixed anhydride that can be reacted with NaN3/DMF solution at similar temperature. Formula 16 can be prepared according to WO2008112408.
The present invention relates to the compound of Formula I and the method preparing Formula I according to Process E.
##STR00007##
Wherein
R1 is selected from H, halogen, halogeno-C1-C6alkyl, C1-C6alkyl, C1-C6alkoxy, cyano or nitro;
R2 is selected from C1-C6alkoxy, or nitro.
Process E of the invention comprises preparing Formula I, a preferred procedure is shown in Scheme VI via acylation of Formula VIII with methylamine hydrochloride with heat pre-activation of formula VIII at the presence of CDI gives Formula I, preferably the reaction is carried out in DMF or dioxane for 2-8 hours with 1.5-4 eq CDI at 50-120° C. Formula VII can be similarly prepared by reacting formula 19 with Formula VI with a base, such as: Na2CO3, Cs2CO3 or K2CO3, or with Formula V in one pot KI or NaI with a base, such as: Na2CO3, Cs2CO3 or K2CO3, as described in Scheme III. Formula VIII can be prepared by hydrolysis of Formula VII under a strong basic condition, such as a mixture of an aqueous NaOH solution and EtOH. Formula 19 can be prepared according to WO2008112408 from formula 18.
The present invention relates to the compound of Formula I or Formula II and the method preparing Formula I or Formula II according to Process F.
##STR00008##
##STR00009##
Wherein
R1 is selected from H, halogen, halogeno-C1-C6alkyl, C1-C6alkyl, C1-C6alkoxy, cyano or nitro;
R2 is selected from C1-C6alkoxy, or nitro.
Process F of the invention comprises preparing Formula I, a preferred procedure is shown in Scheme VII via:
(a) Coupling formula 11 with Formula IX at 100-160° C. in lutidine, such as 1,6-lutidine, or pyridine with 1.5-3 eq DMAP for 2-24 hours gives Formula I, or
(b) coupling formula 11 with Formula IX under similar Ullmann reaction conditions, such as: a base of Na2CO3, Cs2CO3 and K2CO3 with catalytic amount of CuI (1-50% eq) and 2-piclinic acid (1-50% eq) at 100-160° C. in DMF or NMP for 10-36 hours gives Formula I, or
(c) coupling formula 11 with Formula IX under similar Ullmann reaction conditions, such as: a base of Na2CO3, Cs2CO3 and K2CO3 with catalytic amount of CuI (1-50% eq) and pentanedione (1-50% eq), such as 1,4-pentanedione, at 100-160° C. in DMF or NMP for 10-36 hours gives Formula I.
Formula IX can be prepared by reacting Formula IV with formula 21 under Mitusnobu reaction condition in THF at 0-40° C. for 2-24 hours by use of Mitusnobu reagents, such as: DEAD or DIAD at the presence of a Mitsunobu ligand, such as triphenylphosphine. Formula 21 can be prepared by deprotection of formula 20 with TFA at 60-100° C. for 0.5-8 hours to give a TFA salt that can be neutralized by aqueous NaHCO3 solution, and then filtered off.
Process F of the invention comprises preparing Formula II, a preferred procedure is shown in Scheme VIII via:
(a) Coupling formula 11 with formula 21b at 100-160° C. in lutidine, such as 1,6-lutidine, or pyridine with 1.5-3 eq DMAP for 2-24 hours gives Formula II, or
(b) coupling formula 11 with formula 21b under similar Ullmann reaction conditions, such as: a base of Na2CO3, Cs2CO3 and K2CO3 with catalytic amount of CuI (1-50% eq) and 2-picolinic acid (1-50% eq) at 100-160° C. in DMF or NMP for 10-36 hours gives Formula II, or
(c) coupling formula 11 with formula 21b under similar Ullmann reaction conditions, such as: a base of Na2CO3, Cs2CO3 and K2CO3 with catalytic amount of CuI (1-50% eq) and pentanedione (1-50% eq), such as 1,4-pentanedione, at 100-160° C. in DMF or NMP for 10-36 hours gives Formula II.
Formula 21b can be prepared by reacting formula 15c with formula 21 under Mitusnobu reaction condition in THF at 0-40° C. for 2-24 hours with use of Mitsunobu reagents, such as: DEAD or DIAD, at the presence of a Mitsunobu ligand, such as triphenylphosphine.
The present invention relates to the methods of preparing a crystalline form of 6-(7-((1-aminocyclopropyl)-methoxy)-6-methoxyquinolin-4-yloxy)-N-methyl-1-naphthamide (AL3810) by recrystallizing the crude product from isopropanol to give a stable crystalline form. The crude product was dissolved at refluxing condition for 15 minutes to 3 hours in isopropanol with certain amount of active carbon. The reaction was filtered at hot condition and cooled to room temperature (optionally cooled at 4° C.) for 4 to 48 hours. The precipitate was filtered and dried under high vacuum at 25° C.-80° C. to give a stable crystalline form with melting point at 185° C.-205° C. The crystalline form has no observable endotherm from about 40° C. to about 185° C. as determined by DSC. It has observable endotherm from about 185° C. to about 210° C. as determined by DSC. The crystalline form has a TGA thermogram that doesn't exhibit significant weight loss until at 210° C. to 250° C. to indicate that it is an unsolvated material. The crystalline form has 20-40 characteristic peaks on XRPD graph.
The following examples further illustrate the present invention, but should not construed as in any way to limit its scope.
To a stirred mixture of 4-methoxybenzyl 1-((6-methoxy-4-(5-(methylcarbamoyl)-naphthalen-2-yloxy)-quinolin-7-yloxy)methyl)cyclopropylcarbamate Formula II (150 g) in DCM (1.5 L) was added TFA (150 ml) through an additional funnel for about 30 min at RT. The reaction was stirred at 30° C. for 4 hours and added into water (3 L). The aqueous layer was extracted with DCM twice (1.5 L×2) and basified with 3N NaOH (620 ml) to adjust pH 11-12 with a fine white solid precipitation. The solid was filtered and washed with water, further suction dry. The solid was dissolved into a mixture of chloroform/methanol (5 L, 3.5 L/1.5 L) and further washed with brine (2 L). It was dried with MgSO4 and filtered. The solution was evaporated with EtOAc (2 L) three times to a slurry solution and cooled to RT. It was filtered and the filter cake was washed with ether, further air dried to give the crude titled compound 105 g, yield: 95.9%. MS: (M+1) 444.
To a stirred mixture of 4-methoxybenzyl 1-((6-methoxy-4-(5-(methylcarbamoyl)naphthalen-2-yloxy)-quinolin-7-yloxy)methyl)cyclopropylcarbamate Formula II (1 g) in ACN (15 ml) was added TSA.H2O (3 eq). The reaction was stirred at RT for 24 hours and it was basified with 3N NaOH. The solution was extracted with DCM three times, washed with brine and dried with MgSO4. The solution then was filtered and evaporated, further recrystallized from IPA to give pure titled compound 550 mg, yield: 75%. MS: (M+1) 444.
##STR00010##
To a stirred mixture of 6-hydroxy-1-naphthoic acid (19 g, formula 10) in DMF (150 ml) was added CDI (22 g). The reaction was heated at 80° C. for 30 min and CH3NH2.HCl (40 g) was added into the reaction. The reaction was heated for 3 hours at 80° C. and cooled to RT and further diluted with water (300 ml). It was acidified with 1N HCl to pH 2-3 and extracted three times with EtOAc (150 ml). The combined organic layer was washed with saturated NaHCO3 solution followed by water and brine. The solution was dried with Na2SO4 and evaporated to give the 4-hydroxy-N-methyl-naphamide formula 11 compound 12 g.
##STR00011##
(i) To a mixture of formula 11 (6.5 g), formula 12 (6.5 g) and DMAP (5.5 g) was added 1,6-lutidine (20 ml). The reaction was stirred and heated at 135° C. for 5 hours from heterogeneous to homogeneous. The reaction was cooled and IPA (35 ml) was added into the reaction under slow stirring for 2 hours at RT. The solid was filtered and further washed with IPA, dried to give the formula 13 compound 5.8 g as a gray solid, yield 57%, or
(ii) To a mixture of formula 11 (500 mg), formula 12 (500 mg), CuI (80 mg), Cs2CO3 (1 g) and 1-picolinic acid (150 mg) was added DMF (0.5 ml). The reaction was stirred and heated at 120° C. for 24 hours. It was directed loaded on silica gel column to purify to give the formula 13 compound 370 mg, yield 48%, or
(iii) To a mixture of formula 11 (500 mg), formula 12 (500 mg), CuI (80 mg), Cs2CO3 (1 g) and 2,4-pentanedione (10 mg) was added DMF (0.5 ml). The reaction was stirred and heated at 120° C. for 24 hours. It was directed loaded on silica gel column to purify to give the formula 13 compound 450 ma, yield 58%.
##STR00012##
A mixture of formula 13 (5.8 g) and TFA (12 ml) was heated at 90° C. for one hour. The reaction was evaporated under reduced pressure and triturated with EtOAc. The solid was filtered and washed with EtOAc twice to give formula 14 as a TFA salt 5.5 g, yield 95%.
##STR00013##
To a mixture of acid-ester (8.2 g, formula 15) and 4-methoxybenzyl alcohol (9.5 g) in toluene (50 ml) was added DPPA (15 g), the reaction was stirred and TEA was added into the reaction through an additional funnel at RT. The reaction then was refluxed for 20 hours and cooled to RT. To the reaction was added 2N NaOH (30 ml) and followed by extraction with EtOAc three times. The combined organic layer was washed with water to neutral and dried with Na2SO4. The solution was filtered and evaporated followed by addition of EtOAc/PE (petroleum ether) and stored in a refrigerator overnight. The crystals were filtered and washed with cold EtOAc/PE to give an off white powder. The product formula 15b was vacuum oven dried at 30° C. to give 8.0 g as ethyl 1-((4-methoxybenzyloxy)carbonylamino)cyclopropanecarboxylate (formula 15b), yield: 53%. MS: (M+1) 294.
##STR00014##
To a mixture of formula 15b (8.0 g) and THF (50 ml) was added NaBH4 (8 g). The reaction was refluxed for 12 hours. Methanol (15 ml) was slowly added to the reaction and refluxed for 4 hour. The solvent was evaporated and cooled. NH4Cl (6.3 g) and water (60 ml) were added and stirred. The mixture was extracted with DCM three times and dried with Na2SO4. The solution was filtered and evaporated followed by addition of ethanol to recrystallize overnight. The crystal was filtered to give an off white powder and further dried in oven to give the product 4.0 g as 4-methoxybenzyl 1-(hydroxymethyl)cyclopropylcarbamate (formula 15c), yield: 58%. MS: (M+1) 252.
##STR00015##
To a stirred mixture of formula 15c (100 g) and DCM (400 ml) was added DIPEA (78 g). The result solution was cooled to 0-5° C. with ice/water and further stirred under this temperature for 15 min. MsCl (60 g) was added via an addition funnel dropwise keeping temperature below 5° C. for about 1.5 hours. After completion of addition, the reaction mixture was allowed stirring at 0-5° C. for 30 min and quenched with saturated NaHCO3 (300 ml). The solution was extracted with 200 ml DCM twice. The combined DCM layer was washed with 0.1 N HCl (400 ml) followed by brine. It was dried over Na2SO4 and concentrated to obtain an off-white solid 123 g of formula 15d, MS: (M+1) 330.
##STR00016##
To a stirred mixture of formula 15d (3.3 g) and KI (3.3 g) was added acetone (30 ml), the reaction was refluxed for 2 hours and cooled. The reaction was evaporated and extracted with EtOAc (30 ml) twice and washed with brine, further evaporated under reduced pressure to give the crude product 2.3 g of formula 15e, MS: (M+1) 362.
##STR00017##
Method A:
To a stirred mixture of formula 14 (500 mg), formula 15d (450 mg), K2CO3 (400 mg) and NaI (180 mg) was added acetone (10 ml), the reaction suspension was heated to reflux for 20 hours as one pot reaction. The reaction was evaporated and purified on silica gel column to give the product 510 mg of Formula II. MS: (M+1) 608. 1H NMR (DMSO-d6): δ: 8.53-8.54 (m, 2H), 8.37-8.39 (d, 1H), 8.00-8.02 (d, 1H), 7.83-7.88 (m, 2H), 7.53-7.61 (m, 4H), 7.42 (s, 1H), 7.22-7.24 (d, 2H), 6.83-6.85 (d, 2H), 6.61-6.62 (d, 1H), 4.91 (s, 2H), 4.23 (s, 2H), 3.95 (s, 3H), 3.70 (s, 3H), 2.86-2.87 (d, 3H), 0.83-0.93 (d, 4H).
Method B:
To a stirred mixture of formula 14 (500 mg), formula 15e (500 mg) and K2CO3 (400 mg) was added acetone (10 ml), the reaction suspension was heated to reflux for 20 hours. The reaction was evaporated and purified on silica gel column to give the product 560 mg of Formula II. MS: (M+1) 608. 1H NMR conforms to Formula II from above Method A.
Method C:
To a stirred mixture of formula 14 (33 g), formula 15d (43 g), K2CO3 (41 g) and KI (16.6 g) was added acetone (400 ml). The reaction suspension was heated to reflux for about 30 hr. The reaction was concentrated and to the residue was added water (700 ml). The result suspension was stirred for 1 hour slowly to get a brown solid. The solid was filtered and rinsed with water twice further rinsed with ethanol. The crude product was dried in oven at 40° C. for 2-3 hours. The product was purified with IPA by recrystallization to give 29 g of Formula II. MS: (M+1) 608. 1H NMR conforms to Formula II from above Method A.
A mixture of 2-(1-((6-methoxy-4-(5-(methylcarbamoyl)naphthalen-2-yloxy)quino-lin-7-yloxy)methyl)cyclopropyl)acetyl azide formula 17 (WO2008112408, 150 mg) and 4-methoxybenzyl alcohol (0.15 ml) in toluene (10 ml) was refluxed for 1.5 hour. The reaction was evaporated and purified with silica gel column to give the titled product. Mass: (M+1), 608
##STR00018##
A mixture of 6-Hydroxy-1-naphthoic acid (1 g) and H2SO4 (0.2 ml) in EtOH (25 ml) was refluxed overnight and evaporated, followed by dissolving into EtOAc. The solution was washed with water, 1N NaHCO3 solution and brine, further dried by Na2SO4. The solution was evaporated to give crude ethyl 6-hydroxy-1-naphthoate 0.9 g which was reacted with formula 12 at similar preparation conditions to formula 13 of Example 3 to give the above product of formula 18. Formula 19 was similarly prepared to formula 14 of Example 3.
A reaction between formula 19 and formula 15d similarly to the preparation of Formula II of Method A gave ethyl 6-(6-methoxy-7-((1-((4-methoxybenzyloxyl)carbonylamino)cyclopropyl)methoxy)quinolin-4-yloxy)-1-naphthoate which was hydrolyzed with 10% NaOH in EtOH at RT to give 6-(6-methoxy-7-((1-((4-methoxybenzyloxy)carbonylamino)cyclopropyl)methoxy)-quinolin-4-yloxy)-1-naphthoic acid. The resulting acid was acylated similarly to the preparation of formula 11 of Example 3 with CH3NH2.HCl under the heat pre-activation at the presence of CDI to give the titled product.
##STR00019##
To a mixture of 4-chloro-6-methoxyquilolin-7-ol (formula 21, 5.2 g), 1-((4-methoxybenzyloxy)carbonylamino)cyclopropanecarboxylate (formula 15b, 8.3 g) and triphenylphosphine (9.8 g) in THF (250 ml) was added DEAD (6.5 g) dropwise at RT in 1.5 hours, the reaction was further stirred for 20 hours at RT and evaporated. The residue was purified with silica gel column to give the 4-methoxybenzyl 1-((4-chloro-6-methoxy-quinolin-7-yloxy)methyl)cyclopropylcarbamate formula 21b product 6.5 g.
The titled compound of Formula II was then similarly prepared by using formula 21b to react with 4-hydroxy-N-methyl-naphamide formula 11 according to formula 13 of Example 3.
The crude product from Example 1 (105 g) was mixed with isopropanol (2.5 L) and active carbon (5 g), the mixture was heated to reflux for 0.5 hour to dissolve all crude product followed by filtration while it was hot, then the filtrate was refluxed again for 10 minutes and it was cooled to room temperature overnight under a slow stirring condition. The precipitate was filtered and washed with ethyl ether (500 ml×2), further dried under high vacuum at 80° C. to give the pure product (85 g) with melting point at 192° C.-196° C.
H1 NMR shown in
DSC shown in
TGA shown in
XRPD shown in
NO.
Angle
d value
1
10.429
8.476
2
11.811
7.487
3
12.287
7.198
4
13.293
6.655
5
13.658
6.478
6
15.778
5.612
7
16.186
5.472
8
16.682
5.310
9
17.102
5.181
10
17.907
4.949
11
18.631
4.759
12
19.027
4.661
13
19.847
4.470
14
20.545
4.320
15
21.214
4.185
16
21.843
4.066
17
22.058
4.026
18
22.682
3.917
19
23.453
3.790
20
24.065
3.695
21
24.708
3.600
22
25.072
3.549
23
25.435
3.499
24
25.886
3.439
25
27.929
3.192
26
28.420
3.138
27
29.137
3.062
28
30.331
2.944
29
31.172
2.867
30
31.803
2.811
31
32.613
2.743
32
37.959
2.369
33
39.470
2.281
And
H1 NMR shown in
DSC shown in
TGA shown in
XRPD shown in
NO.
Angle
d value
1
10.429
8.476
4
13.293
6.655
6
15.778
5.612
7
16.186
5.472
10
17.907
4.949
12
19.027
4.661
13
19.847
4.470
15
21.214
4.185
16
21.843
4.066
17
22.058
4.026
18
22.682
3.917
19
23.453
3.790
20
24.065
3.695
21
24.708
3.600
22
25.072
3.549
23
25.435
3.499
25
27.929
3.192
31
32.613
2.743
33
39.470
2.281
| Patent | Priority | Assignee | Title |
| Patent | Priority | Assignee | Title |
| 8163923, | Mar 14 2007 | Advenchen Laboratories, LLC | Spiro substituted compounds as angiogenesis inhibitors |
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